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Collagen II mouse Monoclonal Antibody(1H1), 20ul Immune Repertoire Sequencing Three transcript variants encoding two

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Collagen II mouse Monoclonal Antibody(1H1), 20ul Immune Repertoire Sequencing Three transcript variants encoding twoThis gene encodes the alpha 1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye. Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type. In addition, defects in processing chondrocalcin, a calcium

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Description

Three transcript variants encoding two different isoforms have been found for RBBP8

It activates its own transcription which may stabilize commitment to myogenesis

It interacts with the centrosomal proteins aurora-A and ajuba and is required for accumulation of gamma-tubulin and spindle formation at the onset of mitosis

it is expressed at high levels in peripheral blood leukocytes

GO annotations related to this gene include amino acid transmembrane transporter activity and basic amino acid transmembrane transporter activity

Collagen II mouse Monoclonal Antibody(1H1), 20ul Immune Repertoire Sequencing Three transcript variants encoding twoThis gene encodes the alpha 1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye. Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type. In addition, defects in processing chondrocalcin, a calcium

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